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Neural probes are essential tools for the study of neural networks and brain function. While silicon-based probes offer high-electrode density and precise recordings, their high fabrication cost and complex packaging requirements limit scalability and accessibility. Flexible neural probes utilizing flexible printed circuit board (FPCB) technology have emerged as a cost-effective alternative, but their low electrode density, attributed to process limitations, remains a challenge. Herein, we present a fabrication-optimized, flexible neural probe with enhanced electrode density. By optimizing line width and spacing, we considerably increased electrode density while maintaining compatibility with standard FPCB processes. A stiffener layer was incorporated to improve substrate planarity, and a 20% overetching technique was applied to enhance pattern fidelity and reliability. These optimizations tripled the recordable neural signals while maintaining high-signal quality, with a fabrication yield of 73% (200 samples). The fabricated probe demonstrated electrical and mechanical stability and successful in vivo neural recordings. This cost-effective, scalable probe improves accessibility for neuroscience research, particularly in resource-limited settings. This optimized neural probe will contribute to broader and more efficient neural network investigations.
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http://dx.doi.org/10.1021/acsomega.5c02700 | DOI Listing |
Nanoscale
September 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, Jiangsu, China.
Proton exchange membrane water electrolysis (PEMWE) is regarded as the most promising technique for the sustainable production of green hydrogen due to its multiple advantages such as high working current density and high hydrogen purity. However, the anodic oxygen evolution reaction (OER) has a significant impact on the overall efficiency of the electrolytic water reaction due to its sluggish kinetics, which has prompted the search for catalysts possessing both high activity and durability. Iridium oxide exhibits excellent stability under acidic conditions but has poor catalytic activity, leading to its inability to meet the strict requirements of large-scale industrial applications.
View Article and Find Full Text PDFDalton Trans
September 2025
Department of Chemistry, University of Zululand, Private Bag X1001, KwaDlangezwa 3880, South Africa.
To overcome the potential issue of active site blockage by surfactants in colloidal synthesis, alternative synthetic approaches must be explored. In this study, we investigated both solvent-free and colloidal thermolysis routes to synthesize nickel sulfides (NiS and NiS) using sulfur-based Ni complexes, [Ni(SCO(CH))] (Ni-Xan) and [Ni(SCN(CH))] (Ni-DTC) as precursors. The solvent-free decomposition of these complexes produced ligand-free NiS and NiS in the absence or presence of triphenylphosphine (TPP), respectively.
View Article and Find Full Text PDFSmall
September 2025
School of Mechanical Engineering, Yonsei University, 50, Yonsei-ro, Seodaemun-gu, Seoul, 03722, Republic of Korea.
Core-shell electrodes provide a potential and innovative approach for significantly enhancing the performance and capacity of supercapacitors (SCs) by combining two distinct materials. The capabilities of these advanced electrodes surpass those of conventional single electrodes. Specifically, these exhibit better energy storage, higher power density, and improved overall performance.
View Article and Find Full Text PDFACS Electrochem
September 2025
Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom.
The surface structure of an electrocatalyst plays a crucial role in determining the activity. As a model system, gold has been widely investigated as an electro-oxidation catalyst, although there has been much less research on the oxygen evolution reaction (OER) in the potential region of gold oxidation. Here, we combine voltammetric scanning electrochemical cell microscopy (SECCM) and electron backscatter diffraction (EBSD), at different spatial and angular resolutions, respectively, to correlate the local crystallographic structure of polycrystalline goldfocusing on grains close to (113), (011), (114), and (111) orientationswith the electrocatalytic behavior for the OER.
View Article and Find Full Text PDFACS Electrochem
September 2025
Liquid Sunlight Alliance, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.
Reaction rate coefficients for electron-transfer processes at the electrode-electrolyte interface are commonly estimated by using the Butler-Volmer equation, but their values are inaccurate beyond a few tenths of volts of overpotential. The Marcus-Hush-Chidsey (MHC) formalism yields correct asymptotic behavior of the rate coefficients vs applied overpotential but has complex dependencies on the redox system's intrinsic parameters, which can be difficult to model or measure. In this work, we bridge the two kinetics formalisms to estimate the reorganization energy, one of the important parameters for the MHC formalism, and investigate its dependence on other intrinsic parameters such as activation barriers, electronic coupling strength, and the density of states of the electrode surface.
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